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KEMILO FT3 Kit - Indonesia BPOM Medical Device Registration

KEMILO FT3 Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221603. The device is manufactured by GOLDSITE DIAGNOSTICS INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.

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BPOM Registered
Risk Class Kelas Resiko : B
KEMILO FT3 Kit
Analysis ID: AKL 20101221603

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SUMIFIN CITRA ABADI

AR Address

Jl. Alam Sutera Boulevard Alam Sutera Town Center (ASTC) Blok 10D No.19, Kel. Pakulonan, Kec. Serpong Utara - Tangerang Selatan 15325

Registration Date

Sep 29, 2022

Expiry Date

May 15, 2025

Product Type

Clinical Chemistry Test System

Total triiodothyronine test system (kit & cair)

Invitro Diagnostics

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